New to this and it is hitting me that it is a waiting game.

Namaste @LisaJHM. I just got back from two weeks in India where I've been saying it many times a day!

Never apologise for dark humour on this site! It is a very human response to times of great stress and trouble. We have some veritable experts of dark jokes in the face of cancer here, and we're an appreciative audience!

@Blossom1961 is right about the shower on the bald head. It's sensational! I tried the cold cap but it didn't work well enough for me to persist so I gave it away after two rounds and went the chop. Very freeing, and everyone said it looked great. My husband called me his "sexy alien"!

Hope you're having a good Christmas Day. K xox

@LisaJHM For your friend's wedding, you could rock a beautiful turban.  :)

@LisaJHM Yep. Small chunks. I couldn’t take it all in at once and I actually didn’t want to know the stage as I felt that was too daunting. Once chemo was finished I asked them and I was a stage 2B. Just deal with one step at a time. If you want to know ask. Write down questions as you think of them because you will definitely forget them once you are in the appointment. Your hospital may have a wig library so check that out and have fun trying on all the different styles. I was laughing so hard and my daughter who came with me kept looking at me cross eyed. In the end I decided bald is beautiful. Wait until you feel the shower on your bald head - absolutely liberating (almost orgasmic, oops). 

Hi Everyone thank you so much for the kind words and advice.

By a miracle I got into to see the oncologist I wanted (and my surgeon recommended in the public system) yesterday - on Thursday the clinic staff (and I understand they are under a lot of pressure) said no she wasn't available and that I would be seeing the old professor (who turns out was retiring - which they didn't tell me) and that the oncologist I wanted to see wasn't a breast specialist (which again isn't true - found out after I rang my surgeon to report what was going on). So Thursday was a very black day. I ranted and raved and cried finally to let it all out (not at the staff, in the car by myself) .

By some miracle on Friday morning the clinic rang back and said that my preferred oncologist would take me on and could I come in at 12. You're right about the oncologist appointment being overwhelming, my god! So looks like I'm up for 6-8 rounds of chemo - every 2 weeks for the first 4 and then every week for the last part.  The tumour is bigger at the moment - which the Dr thinks because I've had a core biopsy (with significant swelling and bruising) followed up a week later with the chip implant (ouch!!!!) which has left it swollen. - it can't have doubled in size in a week!  

On Monday I have to have my lymph node biopsied (again triple ouch as they can't put local anaesthetic in the site) - the Dr couldn't understand why this wasn't done in the original biopsy but c'est la vie. Also getting a breast MR - the Dr was amazing and convinced the imaging specialist it had to be done before Christmas (he was not happy and could hear him yelling on the phone). The $600 out of pocket for that is a huge hit and I have very kind family who are going to pay for it. Being a single parent isn't always the easiest and especially when illness is involved. I'm lucky that my daughter will be with her father this year for Christmas so she won't have to accompany me to all these appointments. 

So my next couple of weeks look like this - 24th breast MR/node biopsy, 27th bone scan and CT, 31st followup appt with Dr and then likely start 2 or 3 Jan.  I am going to ask for the cold cap although the Dr said it likely wouldn't work as they are going to hit it hard in the first 2 rounds. She recommended I get my hair cut short asap (try finding a hair dresser who isn't 1. manically busy and 2. open between Christmas and New Years). I've got collar bone thick hair and a very round face - I'm hoping I won't end up looking like Bert Newton :) - particularly as I have a friend's wedding on 2 Feb. But alas that's not what is important, wellness is. Sorry I jest when overwhelmed. 

I am attempting to make the most of the next week and enjoy myself as know the road ahead is going to be bumpy.  I have started using the term Namaste - I'm not any religion or particularly involved in yoga but when I read what it means it seems really appropriate.
Namaste :smile:

@Nefertari  I got my path results at the beginning of January this year (which sent me back into surgery on 8/1).  I had a 4.5cm lobular tumour which turned out to have spread to 3 nodes (1 fully gone and 2 with micrometastases) but no further spread, OR & PR+ HER-.  I don't remember either my surgeon or onc telling me what stage I was and, from what I read, it could have been either.  It was only at my recent 12 month appointment with the surgeon that I asked him, "By the way..."  It turns out that I'm at Stage II but from the tone of his response, though he was happy to tell me, he didn't seem to think it was that important.  I'm inclined to agree with him as I don't think there's too much distinction between the 2 stages for me but you do feel a bit of a dill when someone asks you and you have to say that you don't know.

Hi @Nefertari, to answer your lymph node question. I had a few removed during surgery. I was given the option of paying approx $500 (private hospital) to have them tested while I was still under. This meant that they brought two people in to the hospital to do the tests on the spot. If they were positive for cancer in the lymph nodes then they would have continued the surgery and removed all the lymph nodes.  However the results (because they are done so quickly) are only 50% accurate. This means if the initial testing is negative, it may still change to a positive over the next week. Mine was negative. Seven days later when I went back to the surgeon for the results from the surgery, they were still negative. So that was lucky for me.  All the very best. The waiting becomes very consuming of your emotions. Come to this site and everyone will help you through. I practically lived on here during the first few weeks, and the overwhelming love and support from everyone here is what got me through xxx

Hi Sister :) all I know  is it  hasn't spread to bones or any where else, so i have been told.
 I did ask surgeon he said 3 and masectomy but now oncologist  said 2  to 3 , due to the  size and I'm triple negative. He has doubts the second lesion is non malignant. 
 I am completly ignorant because everyone's situation is different and their treatment is in different orders.
Oddly it seems that it is the first question people ask me all the time and I truly don't know?
 I sort of get the impression it will depend on if the lymph nodes have cancer and I dont know when that happens. 
Did you find out post surgery?
I'm just concentrating on one visit at a time.
One chemo down, next is the port on Monday, then  rebiopsy the second lesion again on Thursday. Oncologist wants it done again, he said because of the triple negative result. My head was literally in another world by then far far
Away....
Then I  finally have  two weeks break from hospital before second chemo cycle. 
 I am better dealing with small chunks rather than the big picture.
Nothing has been as bad as I expected so far, the frustration is only that the appointnents never start on time!
 So hurry up and wait fits my experience perfectly. 
The upside is I get to talk to lots of lovely ladies at various stages on the journey.  Made some good friends already...seen everyones ports etc they are all positive ladies regardless of the Stage.

@Nefertari I only found out about my staging 12 months later.  I knew I wasn't 1 nor was I IV and I don't think the docs  really seem to think it mattered.

Welcome @LisaJHM

Some great advice already from everyone as usual.

There is nothing that prepares you for that earthshattering diagnosis.  The fear that surfaces at the start is indescribable and  nobody  can truly understand unless they have felt it.  I remember each morning waking up hoping it had all been a horrible dream, unfortunately not. 

Waiting, waiting , waiting for scans, waiting for results, waiting for doctors that run late all the time.  Frustrating, annoying and frightening...absolutely.  Too much time to think.  

I think one of the worst parts at the beginning was feeling like you have no control.   Don't be scared to ask questions and don't be scared to say so if you don't like something and tell them if you don't quite understand.  This is your gig.

I did surgery first then the chemo and rads.  After the diagonsis I found the first oncology appointment to be the most daunting, scared the bejeesus out of me actually.
  Just remember, they will give you a list a mile long of possible side effects. Doesn't mean you will get them.  Some of us get through without too many problems.

Are you able to access a cold cap for your hair where you are going? 

I always recommed to take photos of all the good things you do amongst navigating treatment.  That way when you look back that part of your life is not all about the cancer and treatment.

In the meantime, keep yourself busy, distraction can work wonders.

You got this lovely. Hugs.

xoxoxox






 

Hi LisaJHM, I'm newly disgnosed 11th Dec.

I understand the frustration! From the mammogram and being told by GP it was most likely cancer (3 areas in same breast),  it took 3 weeks to get into the clinic (public), I was told it would be one week.  I was so frustrated which is rare for me that I rang my GP to vent and he called the them.  Voila they rang within an hour with an appointment time, so try that it can't hurt. 

Once I was "in" though things happened fast and they are all awesome.  

I love <3 that saying AllyJay "Hurry up and wait" it says it all really. 

On the positive side I now feel that things are happening so fast :p   An appointment /scan/ test every day and no free days to be myself. 

I thought I had a four day break but I just got a call that the portacath is booked for Christmas Eve and they want to redo a biopsy on the 27th December that was said not to be cancer.  I was told only one lymph node near the tumour was affected but because I'm triple negative my oncologist has advised it.  I don't even know what all that means, nor do I know my stage cancer as they have mentioned 11 and 111.  I take it one day at a time and do the things I love, spend time with the positive people and of course my animals.

I had my first chemo yesterday and it was not as bad as I expected, lovely nurses and environment and I am feeling okay. 
Less anxious now I know what that is like.  Also met a lovely lady at the Clinic who lives near me and we are meeting up after Christmas for coffee, she is further along in treatment and her insights and texts have been fantastic and uplifting, I hope you have the same experience.

This is a very welcoming place and everyone has been more than supportive.